Mutation

Primary Site >> Stomach Cancer

Gene >> AJAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378190
Start	4769904:4769904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774959047
CDS Mutation	c.881T>C
AA Mutation	p.Ile294Thr(p.I294T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378190
Start	4712619:4712619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749T>G
AA Mutation	p.Val250Gly(p.V250G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378190
Start	4772405:4772405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043C>A
AA Mutation	p.Thr348Lys(p.T348K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378190
Start	4772461:4772461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201524940
CDS Mutation	c.1099G>A
AA Mutation	p.Val367Met(p.V367M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378190
Start	4769901:4769901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878T>C
AA Mutation	p.Val293Ala(p.V293A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4772433:4772433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4772373:4772373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532761720
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4712095:4712095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4712203:4712203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4772406:4772406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747096848
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4712050:4712050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4711933:4711933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4774445:4774445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564151982
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378190
Start	4772406:4772406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378190
Start	4769932:4769932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.914delA
AA Mutation	p.Asn305IlefsTer148(p.N305Ifs*148)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378190
Start	4712008:4712008(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.141delG
AA Mutation	p.Pro48ArgfsTer105(p.P48Rfs*105)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378190
Start	4769931:4769932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.914dupA
AA Mutation	p.Asn305LysfsTer47(p.N305Kfs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript